WO2000025778A1 - Agonistes de recepteur de 5ht1 et metoclopramide pour le traitement de la migraine - Google Patents

Agonistes de recepteur de 5ht1 et metoclopramide pour le traitement de la migraine Download PDF

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Publication number
WO2000025778A1
WO2000025778A1 PCT/IB1999/001694 IB9901694W WO0025778A1 WO 2000025778 A1 WO2000025778 A1 WO 2000025778A1 IB 9901694 W IB9901694 W IB 9901694W WO 0025778 A1 WO0025778 A1 WO 0025778A1
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WO
WIPO (PCT)
Prior art keywords
migraine
metoclopramide
mammal
receptor agonist
treatment
Prior art date
Application number
PCT/IB1999/001694
Other languages
English (en)
Inventor
George Harry Sands
Original Assignee
Pfizer Products Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BR9914901-0A priority Critical patent/BR9914901A/pt
Priority to SK552-2001A priority patent/SK5522001A3/sk
Application filed by Pfizer Products Inc. filed Critical Pfizer Products Inc.
Priority to CA002348543A priority patent/CA2348543A1/fr
Priority to KR1020017005271A priority patent/KR20010089363A/ko
Priority to EA200100284A priority patent/EA200100284A1/ru
Priority to IL14195799A priority patent/IL141957A0/xx
Priority to PL99347541A priority patent/PL347541A1/xx
Priority to APAP/P/2001/002129A priority patent/AP2001002129A0/en
Priority to EP99971318A priority patent/EP1126840A1/fr
Priority to EEP200100243A priority patent/EE200100243A/xx
Priority to JP2000579219A priority patent/JP2002528497A/ja
Priority to AU59947/99A priority patent/AU5994799A/en
Publication of WO2000025778A1 publication Critical patent/WO2000025778A1/fr
Priority to IS5898A priority patent/IS5898A/is
Priority to NO20012013A priority patent/NO20012013L/no
Priority to HR20010298A priority patent/HRP20010298A2/hr
Priority to BG105534A priority patent/BG105534A/xx
Priority to HK02102736.3A priority patent/HK1040929A1/zh

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents

Definitions

  • the present invention relates to a method of treating migraine in a mammal, including a human, by administering to the mammal a 5HT, receptor agonist in combination with metoclopramide. It also relates to pharmaceutical compositions containing a pharmaceutically acceptable carrier, a 5HT ! receptor agonist and metoclopromide. Examples of agonists of 5HT, receptors are agonists of one or more of the 5HT 1A , 5HT 1B , 5HT 1C , 5HT 1D , 5HT ⁇ E , and 5HT 1F receptors.
  • metoclopramide and 5HT, agonists e.g. eletriptan, rizatriptan, naratriptan, sumatriptan, but excluding zolmitriptan
  • agonists e.g. eletriptan, rizatriptan, naratriptan, sumatriptan, but excluding zolmitriptan
  • 5HT ⁇ agonists would exhibit substantially greater efficacy for the treatment of migraine when administered in combination with metoclopramide, in view of the increased blood levels of the oral 5HTi agonist and the antiemetic and antimigraine action of metaclopramide.
  • Metoclopramide is a benzamide derivative, and, although it is related to the neuroleptics, it has no significant antipsychotic or sedative properties. Metoclopramide is a dopamine and 5HT 3 receptor antagonist and also possesses some 5HT 4 agonist activity. The actions of metoclopramide include antagonism of emesis induced by apomorphine or ergotamine. It also induces hyperprolactinemia, a characteristic of dopaminergic blockade. Metoclopramide has relatively low affinity for the dopamine-2 (D2) receptor.
  • D2 dopamine-2
  • the present invention relates to pharmaceutical compositions for the treatment of migraine in a mammal, including a human, comprising metoclopramide; a 5HTi receptor agonist, or a pharmaceutically acceptable salt thereof, excluding zolmitriptan; and a pharmaceutically acceptable carrier.
  • This invention also relates to a method of treating migraine in a mammal, including a human, comprising administering to said mammal an amount of a pharmaceutical composition comprising metoclopramide; a ⁇ HTi receptor agonist, or a pharmaceutically acceptable salt thereof, excluding zolmitriptan; and a pha ⁇ naceutically acceptable carrier; that is effective in treating migraine.
  • This invention also relates to a method of treating migraine in a mammal, including a human, comprising administering to said mammal metoclopramide; a 5HT ⁇ receptor agonist, or a pharmaceutically acceptable salt thereof, excluding zolmitriptan; in amounts that render the combination of such two active agents effective in the treatment or prevention of migraine.
  • Preferred embodiments of this invention relate to pharmaceutical compositions for the treatment of migraine and methods of treating migraine, as described above, wherein the 5HT ! receptor agonist is selected from eletriptan, naratriptan, rizatriptan, sumatriptan almotriptan, avitriptan, frovatriptan, alniditan, LY 334370, LY 306258, BMS-180048 and BMS-181885.
  • a most highly preferred embodiment is the pharmaceutical combination of eletriptan and metoclopramide wherein it is also expected that the pharmacokintetics of the eletriptan would be enhanced.
  • compositions for the treatment of migraine and methods of treating migraine relate to pharmaceutical compositions for the treatment of migraine and methods of treating migraine, as described above, wherein the 5HTi receptor agonist is a compound of the formula
  • R , R 4 , and Z are selected, independently, from hydrogen, halo (e.g., chloro, fluoro, bromo or iodo), (C ⁇ -C ) alkyl optionally substituted with from one to three fluorine atoms, (C C 4 )alkoxy optionally substituted with from one to three fluorine atoms, and (C 1 -C 4 )alkoxy- (C C 4 )alkyl wherein each of the alkyl moieties may optionally be substituted with from one to three fluorine atoms;
  • halo e.g., chloro, fluoro, bromo or iodo
  • W is -CH 2 -0-(C ⁇ -C 6 ) alkyl wherein the alkyl moiety can be straight or branched; or W is -CH 2 NR 1 R 2 wherein R 1 and R 2 are independently selected from hydrogen and straight or branched (C r C 6 )alkyl; or R 1 and R 2 , together with the nitrogen to which they are attached, form a saturated four membered monocyclic ring or a saturated or unsaturated nonaromatic five to seven 00/25778 repeal P I-C V -T I / / I I B JTC 9 W 9/01694
  • membered monocyclic ring or a saturated or unsaturated nonaromatic seven to ten membered bicyclic ring which may optionally contain one or two heteroatoms in addition to the nitrogen of NR 1 R 2 , wherein said heteroatoms are independently selected from oxygen, nitrogen and sulfur, and wherein from one to three of the ring carbon atoms, or one of the ring nitrogen atoms, may optionally and independently be substituted with straight or branched (C C ) alkyl, straight or branched (CrC- ⁇ ) alkoxy, straight or branched (C ⁇ Cs) alkyl-(C 3 -C 7 ) cycloalkyl, hydroxy, amino, cyano, halo, aryl-(straight or branched (C ⁇ -C 3 ) alkyl) or heteroaryl- (straight or branched (CrC 3 ) alkyl), wherein said aryl is selected from phenyl and naphthyl and said heteroaryl is selected
  • the foregoing patents and patent applications are incorporated herein by reference in their entireties.
  • treating refers to retarding or reversing the progress of, or alleviating or preventing either the disorder or condition to which the term “treating” applies, or one or more symptoms of such disorder or condition.
  • treatment refers to the act of treating a disorder or condition, as the term “treating” is defined above.
  • This invention relates both to methods of treating migraine in which metoclopramide and the 5HT, receptor agonist are administered together, as part of the same pharmaceutical composition, as well as to methods in which these two active agents are administered separately, as part of an appropriate dose regimen designed to obtain the benefits of the combination therapy.
  • the appropriate dose regimen, the amount of each dose administered, and the intervals between doses of the active agents will depend upon the 5HT t agonist being used, the type of pharmaceutical formulations being used, the characteristics of the subject being treated and the severity of the migraine.
  • the 5HT !
  • metoclopramide will be administered orally to an average 70 kg adult human in an amount ranging from about 1 to about 400 mg per day, in single or divided doses, and metoclopramide will be administered in an amount ranging from about 5 to about 125 mg per day, in single or divided doses.
  • Metoclopramide will generally be administered in amounts ranging from about 20 to about 80 mg per day, depending on the severity of the headache and the route of administration.
  • Metoclopramide can be administered orally, intranasally, intravenously, as a rectal suppository or using a "flash" formulation (u_, allowing the medication to dissolve in the mouth without the need to use water.) 00/25778
  • the 5HT, receptor agonists that are employed in the pharmaceutical compositions and methods of this invention, and their pharmaceutically acceptable salts, may be administered alone or in combination with pharmaceutically acceptable carriers or diluents. They may be formulated in a conventional manner using one or more pharmaceutically acceptable carriers. Such compounds may be adminstered orally, buccally, intranasally, parenterally (e.g., intravenously, intramuscularly or subcutaneously) or rectally, or in a form suitable for administration by inhalation or insufflation.
  • the pharmaceutical compositions may take the form of, for example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents __, pregelatinised maize starch, poiyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g.. lactose, microcrystailine cellulose or calcium phosphate), lubricants (e.g., magnesium stearate, talc or silica); disintegrants (e.g... potato starch or sodium starch glycollate); or wetting agents (e.g., sodium lauryl sulphate).
  • the tablets may be coated by methods well known in the art.
  • Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use.
  • Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g., sorbitol syrup, methyl cellulose or hydrogenated edible fats); emulsifying agents (e.g., lecithin or acacia); non-aqueous vehicles (e.g.. almond oil, oily esters or ethyl alcohol); and preservatives (e.g.. methyl or propyl p-hydroxybenzoates or sorbic acid).
  • suspending agents e.g., sorbitol syrup, methyl cellulose or hydrogenated edible fats
  • emulsifying agents e.g., lecithin or acacia
  • non-aqueous vehicles e.g.. almond oil, oily esters or ethyl alcohol
  • composition may take the form of tablets or lozenges formulated in a conventional manner.
  • the 5HT, agonists of the invention and their salts may be formulated for parenteral administration by injection, including using conventional catheterization techniques or infusion.
  • Formulations for injection may be presented in unit dosage form, e.g., in ampules or in multi-dose containers, with an added preservative.
  • the compositions may take such forms 00/25778
  • suspensions solutions or emulsions in oily or aqueous vehicles, and may contain formulating agents such as suspending, stabilizing and/or dispersing agents.
  • the active ingredient may be in powder form for reconstitution with a suitable vehicle, g,, sterile pyrogen-free water, prior to use.
  • a suitable vehicle g,, sterile pyrogen-free water
  • the 5HT t agonists of this invention and their salts may also be formulated in rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter or other glycerides.
  • the active compounds of the invention are conveniently delivered in the form of a solution or suspension from a pump spray container that is squeezed or pumped by the patient or as an aerosol spray presentation from a pressurized container or a nebulizer, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • the pressurized container or nebulizer may contain a 'solution or suspension of the active compound.
  • Capsules and cartridges for use in an inhaler or insufflator may be formulated containing a powder mix of a compound of the invention and a suitable powder base such as lactose or starch.
  • Aerosol formulations for the treatment of migraine in the average adult human are preferably made so that each metered dose or "puff' of aerosol contains 20 ⁇ g to 1000 ⁇ g of the compound of the invention.
  • the overall daily dose with an aerosol will generally be within the range of about 100 ⁇ g to 10 mg.
  • Administration may be several times daily, for example, 2, 3, 4 or 8 times, giving, for example, 1 , 2 or 3 doses each time.
  • the 5-HT, receptor agonist activity of a compound or salt can be measured in in vitro receptor binding assays as described for the 5-HT ⁇ A receptor, using rat cortex as the receptor source and [ 3 H]8-OH-DPAT as the radioligand (D. Hoyer et aJL, Europ. J. Pharmacol., 1985; 118: 13), and as described for the 5-HT 1D receptor, using bovine caudate as the receptor source and [ 3 H]5-HT as the radioligand (R.E. Heuring and S. J. Peroutka, J. Neuroscience, 1987; 7: 894).
  • the in vitro activity of a compound at the 5-HT 1D binding site may be determined according to the following procedure.
  • Bovine caudate tissue is homogenized and suspended in 20 volumes of a buffer containing 50 mM TRIS hydrochloride (tris[hydroxymethyl] aminomethane hydrochloride) at a pH of 7.7.
  • the homogenate is then centrifuged at 45.000G for 10 minutes.
  • the supernatant is then discarded and the resulting pellet resuspended in approximately 20 volumes of 50 mM TRIS hydrochloride buffer at pH 7.7.
  • This suspension is then pre-incubated for 15 minutes at 37°C, after which the suspension is 00/25778 7 rL I "
  • the resulting pellet (approximately 1 gram) is resuspended in 150 ml of a buffer of 15 mM TRIS hydrochloride containing 0.01 percent ascorbic acid with a final pH of 7.7 and also containing 10 mM pargyline and 4 mM calcium chloride (CaCI 2 ).
  • the suspension is kept on ice at least 30 minutes prior to use.
  • the inhibitor, control or vehicle is then incubated according to the following procedure.
  • DMSO dimethylsulfoxide
  • distilled water solution 200 ml of tritiated 5-hydroxytryptamine (2 nM) in a buffer of 50 mM TRIS hydrochloride containing 0.01 percent ascorbic acid at pH 7.7 and also containing 10 mM pargyline and 4 mM calcium chloride, plus 100 nM of 8-hydroxy-DPAT (dipropylaminotetraline) and 100 nM of mesulergine.
  • TRIS hydrochloride containing 0.01 percent ascorbic acid at pH 7.7 and also containing 10 mM pargyline and 4 mM calcium chloride, plus 100 nM of 8-hydroxy-DPAT (dipropylaminotetraline) and 100 nM of mesulergine.
  • bovine caudate tissue 750 ml of bovine caudate tissue, and the resulting suspension is vortexed to ensure a homogenous suspension. The suspension is then incubated in a shaking water bath for 30 minutes
  • the suspension is filtered using glass fiber filters (e.g., Whatman GF/B-filters).
  • the pellet is then washed three times with 4 ml of a buffer of 50 mM TRIS hydrochloride at pH 7.7.
  • the pellet is then placed in a scintillation vial with 5 ml of scintillation fluid (aquasol 2) and allowed to sit overnight.
  • the percent inhibition can be calculated for each dose of the compound.
  • An IC 50 value can then be calculated from the percent inhibition values.
  • the ability of a compound or salt to bind to 5-HT 1A receptors can be determined according to the following procedure. Rat brain cortex tissue is homogenized and divided into samples of 1 gram lots and diluted with 10 volumes of 0.32 M sucrose solution. The suspension is then centrifuged at 900G for 10 minutes and the supernatant separated and recentrifuged at 70.000G for 15 minutes. The supernate is discarded and the pellet re- suspended in 10 volumes of 15 mM TRIS hydrochloride at pH 7.5. The suspension is allowed to incubate for 15 minutes at 37 C C. After pre-incubation is complete, the suspension is centrifuged at 70.000G for 15 minutes and the supernate discarded.
  • tissue pellet is resuspended in a buffer of 50 mM TRIS hydrochloride at pH 7.7 containing 4 mM of calcium chloride and 0.01 percent ascorbic acid.
  • the tissue is stored at -70°C until ready for an experiment. The tissue can be thawed immediately prior to use, diluted with 10 mm pargyline and kept on ice.
  • tissue is then incubated according to the following procedure.
  • Fifty microliters of control, inhibitor, or vehicle (1 percent DMSO final concentration) is prepared at various dosages.
  • 200ml of tritiated DPAT at a concentration of 1.5 nM in a buffer of 50 mM TRIS hydrochloride at pH 7.7 containing 4 mM calcium chloride, 0.01 percent ascorbic acid and pargyline.
  • To this solution is then added 750 ml of tissue and the resulting 00/25778 _ 8 _
  • the agonist and antagonist activities compounds at 5-HT 1A and 5-HT ⁇ D receptors can be determined using a single saturating concentration according to the following procedure.
  • 5-HT 1A receptors Male Hartley guinea pigs are decapitated and 5-HT 1A receptors are dissected out of the hippocampus, while 5-HT 10 receptors are obtained by slicing at 350 mM on a Mcllwain tissue chopper and dissecting out the substantia nigra from the appropriate slices.
  • the individual tissues are homogenized in 5 mM HEPES buffer containing 1 mM EGTA (pH 7.5) using a hand-held glass-Teflon® homogenizer and centrifuged at 35,000 x g for 10 minutes at 4°C.
  • the pellets are resuspended in 100 mM HEPES buffer containing 1 mM EGTA (pH 7.5) to a final protein concentration of 20 mg (hippocampus) or 5 mg (substantia nigra) of protein per tube.
  • the following agents are added so that the reaction mix in each tube contained 2.0 mM MgCI 2 , 0.5 mM ATP, 1.0 mM cAMP, 0.5 mM IBMX, 10 mM phosphocreatine, 0.31 mg/mL creatine phosphokinase, 100 mM GTP and 0.5-1 microcuries of [32PJ-ATP (30 Ci/mmol: NEG-003 - New England Nuclear).
  • Incubation is initiated by the addition of tissue to siliconized microfuge tubes (in triplicate) at 30°C for 15 minutes. Each tube receives 20 mL tissue, 10 mL drug or buffer (at 10X final concentration), 10mL 32 nM agonist or buffer (at 10X final concentration), 20mL forskolin (3 mM final concentration) and 40 mL of the preceding reaction mix. Incubation is terminated by the addition of 100 mL 2% SDS, 1.3 mM cAMP, 45 mM ATP solution containing 40,000 dpm [ 3 H]-cAMP (30 Ci/mmol: NET-275 - New England Nuclear) to monitor the recovery of cAMP from the columns.
  • Compounds can be tested for in vivo activity for antagonism of 5-HT 1D agonist- induced hypothermia in guinea pigs according to the following procedure.
  • mice Male Hartley guinea pigs from Charles River, weighing 250-275 grams on arrival and 300-600 grams at testing, serve as subjects in the experiment.
  • the guinea pigs are housed under standard laboratory conditions on a 7 a.m. to 7 p.m. lighting schedule for at least seven 00/25778 _o_
  • the compounds of the invention can be administered as solutions in a volume of 1 ml/kg.
  • the vehicle used is varied depending on compound solubility.
  • Test compounds are typically administered either sixty minutes orally (p.o.) or 0 minutes subcutaneously (s.c.) prior to a 5-HT 1D agonist, such as [3-(1-methylpyrrolidin-2-ylmethyl)-1H-i ⁇ dol-5-yl]-(3-nitropyridin-3- yl)-amine, which can be prepared as described in PCT publication W093/111 06, published June 10, 1993 which is administered at a dose of 5.6 mg/kg, s.c.
  • 5-HT 1D agonist such as [3-(1-methylpyrrolidin-2-ylmethyl)-1H-i ⁇ dol-5-yl]-(3-nitropyridin-3- yl)-amine
  • each guinea pig Before a first temperature reading is taken, each guinea pig is placed in a clear plastic shoe box containing wood chips and a metal grid floor and allowed to acclimate to the surroundings for 30 minutes. Animals are then returned to the same shoe box after each temperature reading. Prior to each temperature measurement each animal is firmly held with one hand for a 30-second period. A digital thermometer with a small animal probe is used for temperature measurements. The probe is made of semi-flexible nylon with an epoxy tip. The temperature probe is inserted 6 cm. into the rectum and held there for 30 seconds or until a stable recording is obtained. Temperatures are then recorded.
  • a "pre-drug" baseline temperature reading is made at -90 minutes, the test compound is given at -60 minutes and an additional -30 minute reading is taken.
  • the 5-HT 1D agonist is then administered at 0 minutes and temperatures are taken 30, 60, 120 and 240 minutes later.
  • a pre-drug baseline temperature reading is made at -30 minutes.
  • the test compound and 5-HT 1D agonists are given concurrently and temperatures are taken at 30, 60, 120 and 240 minutes later.
  • the 5-HT ⁇ agonist activity can be determined by the
  • the active compounds tested all exhibited an IC 50 in either assay of 1 mM or less.
  • Compounds and salts can be evaluated as anti-migraine agents by testing the extent to which they mimic sumatriptan in contracting the dog isolated saphenous vein strip (P. P. A. Humphrey et aL, B ⁇ > Pharmacol.. 1988; 94: 1128.). This effect can be blocked by methiothepin, a known serotonin antagonist.
  • Sumatriptan is known to be useful in the treatment of migraine and produces a selective increase in carotid vascular resistance in the anaesthetized dog. It has been suggested that this is the basis of its efficacy by Fenwick et aL, British Journal of Pharmacology., 1989; 96: 83.

Abstract

Procédé de traitement de la migraine chez un mammifère, dont un être humain, qui consiste à administrer à ce mammifère un agoniste de récepteur 5HT1, en particulier de l'élétriptan, en combinaison avec du métoclopramide. La présente invention concerne également des compositions pharmaceutiques contenant un excipient acceptable sur le plan pharmaceutique, un agoniste de récepteur 5HT1 et du métoclopramide.
PCT/IB1999/001694 1998-10-30 1999-10-18 Agonistes de recepteur de 5ht1 et metoclopramide pour le traitement de la migraine WO2000025778A1 (fr)

Priority Applications (17)

Application Number Priority Date Filing Date Title
EP99971318A EP1126840A1 (fr) 1998-10-30 1999-10-18 Agonistes de recepteur de 5ht(1) et metoclopramide pour le traitement de la migraine
APAP/P/2001/002129A AP2001002129A0 (en) 1998-10-30 1999-10-18 5HT1 receptor agonists and metoclopramide for the treatment of migrane.
CA002348543A CA2348543A1 (fr) 1998-10-30 1999-10-18 Agonistes de recepteur de 5ht1 et metoclopramide pour le traitement de la migraine
KR1020017005271A KR20010089363A (ko) 1998-10-30 1999-10-18 편두통 치료를 위한 5에이치티1 수용체 작용제 및메토클로프라미드
EA200100284A EA200100284A1 (ru) 1998-10-30 1999-10-18 Агонисты 5ht1 рецепторов и метоклопрамид для лечения мигрени
IL14195799A IL141957A0 (en) 1998-10-30 1999-10-18 5ht1 receptor agonists and metoclopramide for the treatment of migraine
PL99347541A PL347541A1 (en) 1998-10-30 1999-10-18 5ht1
BR9914901-0A BR9914901A (pt) 1998-10-30 1999-10-18 Agonistas do receptor 5ht1 e metoclopramida para o tratamento de enxaqueca
SK552-2001A SK5522001A3 (en) 1998-10-30 1999-10-18 5ht1 receptor agonists and metoclopramide for the treatment of migraine
JP2000579219A JP2002528497A (ja) 1998-10-30 1999-10-18 偏頭痛の治療のための５ｈｔ１受容体アゴニスト及びメトクロプラミド
EEP200100243A EE200100243A (et) 1998-10-30 1999-10-18 5HT1 retseptori agonistid ja metoklopramiid migreeni raviks
AU59947/99A AU5994799A (en) 1998-10-30 1999-10-18 5HT1 receptor agonists and metoclopramide for the treatment of migraine
IS5898A IS5898A (is) 1998-10-30 2001-03-16 5HT1 viðtaka gerandefni og metóklópramíð til meðhöndlunar á mígreni
NO20012013A NO20012013L (no) 1998-10-30 2001-04-24 5HT1 reseptor agonister og metoclopramid for behandling av migrene
HR20010298A HRP20010298A2 (en) 1998-10-30 2001-04-25 5ht<->1<p> receptor agonists and metoclopramide for the treatment of migraine
BG105534A BG105534A (en) 1998-10-30 2001-05-22 5ht1 means and method for the treatment of migraine
HK02102736.3A HK1040929A1 (zh) 1998-10-30 2002-04-11 用於治療偏頭痛的5ht1受體激動劑和甲氧氯普胺

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002070070A2 (fr) * 2001-03-01 2002-09-12 Pfizer Limited Compositions a biodisponibilite renforcee
AU2013202680B2 (en) * 2008-04-28 2016-01-07 Zogenix, Inc. Novel formulations for treatment of migraine

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6579898B2 (en) * 2001-03-01 2003-06-17 Pfizer Inc. Compositions having improved bioavailability
US7645442B2 (en) 2001-05-24 2010-01-12 Alexza Pharmaceuticals, Inc. Rapid-heating drug delivery article and method of use
WO2002094242A1 (fr) * 2001-05-24 2002-11-28 Alexza Molecular Delivery Corporation Administration de rizatriptan ou de zolmitriptan par voie d'inhalation
CA2641760A1 (fr) * 2001-05-24 2002-11-28 Alexza Pharmaceuticals, Inc. Administration par voie pulmonaire d'alprazolam, d'estazolam, de midazolam ou de triazolam
CA2446904A1 (fr) 2001-05-24 2003-04-03 Alexza Molecular Delivery Corporation Administration d'esters medicamenteux par inhalation
US20030051728A1 (en) 2001-06-05 2003-03-20 Lloyd Peter M. Method and device for delivering a physiologically active compound
US20070122353A1 (en) 2001-05-24 2007-05-31 Hale Ron L Drug condensation aerosols and kits
US7498019B2 (en) 2001-05-24 2009-03-03 Alexza Pharmaceuticals, Inc. Delivery of compounds for the treatment of headache through an inhalation route
US7458374B2 (en) 2002-05-13 2008-12-02 Alexza Pharmaceuticals, Inc. Method and apparatus for vaporizing a compound
US7078016B2 (en) 2001-11-21 2006-07-18 Alexza Pharmaceuticals, Inc. Delivery of caffeine through an inhalation route
WO2003041693A1 (fr) * 2001-11-09 2003-05-22 Alexza Molecular Delivery Corporation Administration de diazepam a travers une voie pulmonaire
WO2003094900A1 (fr) 2002-05-13 2003-11-20 Alexza Molecular Delivery Corporation Distribution de medicament a base d'amines par voie d'inhalation
US20040105818A1 (en) 2002-11-26 2004-06-03 Alexza Molecular Delivery Corporation Diuretic aerosols and methods of making and using them
JP2006514934A (ja) 2002-11-26 2006-05-18 アレックザ ファーマシューティカルズ， インコーポレイテッド 疼痛治療用薬剤製造のためのロキサピンまたはアモキサピンの使用
US7550133B2 (en) * 2002-11-26 2009-06-23 Alexza Pharmaceuticals, Inc. Respiratory drug condensation aerosols and methods of making and using them
US7913688B2 (en) 2002-11-27 2011-03-29 Alexza Pharmaceuticals, Inc. Inhalation device for producing a drug aerosol
EP1625336B9 (fr) 2003-05-21 2012-03-21 Alexza Pharmaceuticals, Inc. Utilisation d'une couche de combustible solide, procédé pour fabriquer une telle couche et unité de chauffage correspondante
US7540286B2 (en) 2004-06-03 2009-06-02 Alexza Pharmaceuticals, Inc. Multiple dose condensation aerosol devices and methods of forming condensation aerosols
WO2005123043A2 (fr) * 2004-06-10 2005-12-29 Duramed Pharmaceuticals, Inc. Formulations de sumatriptan absorbables au travers des membranes biologiques, et methodes de production et d'utilisation desdites formulations
US20050282879A1 (en) * 2004-06-17 2005-12-22 Foad Salehani Methods and composition for treatment of migraine and symptoms thereof
DE602006018447D1 (de) 2005-04-13 2011-01-05 Neuraxon Inc Substituierte indolverbindungen mit nos-hemmender aktivität
AR060451A1 (es) * 2006-04-13 2008-06-18 Neuraxon Inc Compuestos de indol 1,5 y 3,6-sustituidos con actividad inhibitoria de nos
US20080139510A1 (en) * 2006-12-07 2008-06-12 Abe Rose Treatment of migraine headaches with sublingual amino acids
WO2008112661A2 (fr) 2007-03-09 2008-09-18 Alexza Pharmaceuticals, Inc. Unité chauffante à utiliser dans un dispositif d'administration de médicament
CN101910157B (zh) * 2007-11-16 2014-05-07 纽尔亚商股份有限公司 吲哚化合物和治疗内脏痛的方法
EP2220074A4 (fr) * 2007-11-16 2012-01-04 Neuraxon Inc Composés d'indole 3,5-substitués ayant une activité d'inhibition de la réabsorption de la nos et de la noradrénaline
WO2009064505A1 (fr) * 2007-11-16 2009-05-22 The Arizona Board Of Regents On Behalf Of The University Of Arizona Procédés de traitement de la douleur viscérale

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2325161A (en) * 1997-05-14 1998-11-18 Merck Sharp & Dohme Pharmaceutical formulation comprising a 5-HT agonist and an anti-emetic and/or gasto-prokinetic agent

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5698571A (en) * 1994-10-05 1997-12-16 Eli Lilly And Company 5-HT1F mediated inhibition of neurogenic meningeal extravasation: a method for the treatment of migraine
BR9710289A (pt) * 1996-07-11 1999-08-17 Farmarc Nederland Bv Composi-Æo farmac-utica contendo sal cido de adi-Æo de medicamento b sico

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2325161A (en) * 1997-05-14 1998-11-18 Merck Sharp & Dohme Pharmaceutical formulation comprising a 5-HT agonist and an anti-emetic and/or gasto-prokinetic agent

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
KELLY A M ET AL: "Intravenous chlorpromazine versus intramuscular sumatriptan for acute migraine.", JOURNAL OF ACCIDENT AND EMERGENCY MEDICINE, (1997 JUL) 14 (4) 209-11., XP000869766 *
ROLAN P: "Potential drug interactions with the novel antimigraine compound zolmitriptan (Zomig, 311C90).", CEPHALALGIA, (1997 OCT) 17 SUPPL 18 21-7. REF: 24, XP000870490 *
SCHWARZBERG M N: "Application of metoclopramide specificity in migraine attacks therapy.", HEADACHE, (1994 JUL-AUG) 34 (7) 439-41., XP000869686 *
SEABER E J ET AL: "The novel anti-migraine compound zolmitriptan (Zomig 311C90) ha no clinically significant interactions with paracetamol or metoclopramide.", EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, (1997) 53 (3-4) 229-34., XP000870485 *
VON SEGGERN R L ET AL: "Cost considerations in headache treatment. Part 2: Acute migraine treatment.", HEADACHE, (1996 SEP) 36 (8) 493-502., XP000869685 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002070070A2 (fr) * 2001-03-01 2002-09-12 Pfizer Limited Compositions a biodisponibilite renforcee
WO2002070070A3 (fr) * 2001-03-01 2003-04-10 Pfizer Ltd Compositions a biodisponibilite renforcee
AU2013202680B2 (en) * 2008-04-28 2016-01-07 Zogenix, Inc. Novel formulations for treatment of migraine
AU2013202680C1 (en) * 2008-04-28 2016-06-23 Zogenix, Inc. Novel formulations for treatment of migraine

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JP2002528497A (ja) 2002-09-03
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CO4950530A1 (es) 2000-09-01
CN1325304A (zh) 2001-12-05
US6255334B1 (en) 2001-07-03
PA8484801A1 (es) 2000-09-29
ZA200103322B (en) 2002-06-10
AP2001002129A0 (en) 2001-06-30
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HK1040929A1 (zh) 2002-06-28
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